mammoScreen
K 號：K192854 · 2020-03-25
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器材摘要
MammoScreen is the device name listed in this FDA 510(k) record. The listed applicant is Therapixel. It received FDA 510(k) clearance on 2020-03-25 under 510(k) number K192854. The device is classified under product code QDQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MammoScreen?
MammoScreen is a medical device that received FDA 510(k) clearance on 2020-03-25. The listed applicant is Therapixel. The 510(k) number is K192854.
When did MammoScreen receive FDA 510(k) clearance?
MammoScreen received FDA 510(k) clearance on 2020-03-25, under 510(k) number K192854.
Who is the listed applicant for MammoScreen?
The FDA 510(k) record lists Therapixel as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MammoScreen?
The FDA product code for MammoScreen is QDQ.
相關臨床試驗
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其他以 Therapixel 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
相關器械（代碼：QDQ）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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